ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "Comparative effectiveness and harms"

  • Abstract Number: L01 • 2019 ACR/ARP Annual Meeting

    Comparative Risk of Hospitalized Serious Infection in Patients with Psoriasis and Psoriatic Arthritis: A Population-Based Multi-Database Study

    Yinzhu Jin 1, Hemin Lee 1, Moa Lee 2, Joan Landon 3, Joseph Merola 4, Rishi Desai 5 and Seoyoung C. Kim1, 1Brigham and Women's Hospital and Harvard Medical School, Boston, 2University of North Carolina Chapel Hill, Chapel Hill, North Carolina, 3Brigham and Women's Hospital, Boston, Massachusetts, 4Harvard Medical School, Brigham and Women's Hospital, Boston, 5Brigham and Women's hospital, Boston

    Background/Purpose: The risk of serious infection when using disease-modifying antirheumatic drugs (DMARDs), including biologic drugs is one of the major concerns for psoriasis/psoriatic arthritis (PsO/PsA)…
  • Abstract Number: 580 • 2018 ACR/ARHP Annual Meeting

    Clinical Effectiveness of Tofacitinib 11mg Once Daily (QD) Versus Tofacitinib 5mg Twice Daily (BID) in the Corrona US RA Registry

    Stanley Cohen1, Heather J Litman2, Connie Chen3, Tatjana Lukic3, Ann Madsen3, Liza Takiya4, Kimberly J Dandreo2, Taylor Blachley2 and Jeffrey Greenberg2, 1Metroplex Clinical Research Center and University of Texas Southwestern Medical Center, Dallas, TX, 2Corrona LLC, Waltham, MA, 3Pfizer Inc, New York, NY, 4Pfizer Inc, Collegeville, PA

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of RA, originally approved at 5 mg twice daily (BID). In 2016, an extended-release…
  • Abstract Number: 604 • 2018 ACR/ARHP Annual Meeting

    Combining Observational and Randomized Controlled Trial Data Evidence to Jointly Estimate Remission and Response for Biologic and Non-Biologic Therapies in Rheumatoid Arthritis: A Bivariate Network Meta-Analysis

    Gyanendra Pokharel1, Rob Deardon1, Cheryl Barnabe2, Vivian P. Bykerk3, Susan J. Bartlett4, Louis Bessette5, Gilles Boire6, Carol Hitchon7, Edward C. Keystone8, Janet E. Pope9, Diane Tin10, Carter Thorne11 and Glen Hazlewood12, 1Department of Mathematics and Statistics, University of Calgary, Calgary, AB, Canada, 2Medicine, University of Calgary, Calgary, AB, Canada, 3Hospital for Special Surgery, New York, NY, 4Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 5Division of Rheumatology, Department of Medicine, CHU de Québec-Université Laval, Québec, QC, Canada, 6Rheumatology Division, Centre intégré universitaire de santé et de services sociaux de l'Estrie - Centre Hospitalier Universitaire de Sherbrooke and Universite de Sherbrooke, Sherbrooke, QC, Canada, 7University of Manitoba, Winnipeg, MB, Canada, 8Mount Sinai Hospital, Toronto, ON, Canada, 9Department of Medicine, University of Western Ontario, London, ON, Canada, 10The Arthritis Program, Southlake Regional Health Centre, Newmarket, ON, Canada, 11University of Toronto, Newmarket, ON, Canada, 12Departments of Medicine and Community Health Sciences, University of Calgary, Calgary, AB, Canada

    Background/Purpose: Remission is the goal of rheumatoid arthritis (RA) treatment, but ACR responses are more commonly measured in clinical trials. As such, data on remission…
  • Abstract Number: 2877 • 2018 ACR/ARHP Annual Meeting

    The Comparative Effectiveness of First-Line Tumor Necrosis Factor Inhibitor (TNFi) Compared with Non-TNFi Agents in Patients with Rheumatoid Arthritis: Results from the Corrona Registry

    Dimitrios A. Pappas1, Gregory St. John2, Carol J. Etzel1, Stefano Fiore3, Taylor Blachley1, Toshio Kimura2, Rajeshwari Punekar3, Kelechi Emeanuru4, Susan Boklage2 and Joel Kremer1,5, 1Corrona LLC, Waltham, MA, 2Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 3Sanofi, Bridgewater, NJ, 4Corrona, LLC, Waltham, MA, 5Albany Medical College and The Center for Rheumatology, Albany, NY

    Background/Purpose: RA patients who are intolerant or have an inadequate response to conventional synthetic DMARDs (csDMARDs) can be treated with a biologic DMARD (bDMARD). Tumor…
  • Abstract Number: 635 • 2017 ACR/ARHP Annual Meeting

    Short-Term Efficacy and Safety of New Biological Agents Targeting the IL-6, IL-12/23 and IL-17 Pathways for Active Psoriatic Arthritis: A Network Meta-Analysis of Randomised Controlled Trials

    Dongze Wu, Jiang Yue and Lai-Shan Tam, Department of Medicine & Therapeutics, The Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, Hong Kong

    Background/Purpose:  According to EULAR recommendations, in patients with peripheral arthritis and an inadequate response to at least one conventional synthetic DMARD, biologic DMARDs targeting IL-12/23,…
  • Abstract Number: 1825 • 2017 ACR/ARHP Annual Meeting

    Comparative Analysis of Achievement of Individual Important Response Measured By DAS28dcrit in a Randomized Head-to-Head Trial of Tocilizumab Vs. Adalimumab in Active Rheumatoid Arthritis

    Michaela Koehm1, Michael Hofmann2, Rasmus Lüthje2, Matthew McIntosh3, Varghese Abraham3, Cem Gabay4, Arthur Kavanaugh5, Harald Burkhardt6 and Frank Behrens6, 1Division of Rheumatology and Fraunhofer IME-Project-Group Translational Medicine and Pharmacology, Goethe University, Frankfurt/Main, Germany, 2Rheumatology, Chugai Pharma Europe Ltd., Frankfurt, Germany, 3Genentech, San Francisco, CA, 4SCQM, Geneva, Switzerland, Geneva, Switzerland, 5Medicine, University of California, San Diego, La Jolla, CA, 6Division of Rheumatology and Fraunhofer IME-Project-Group Translational Medicine and Pharmacology, Goethe University, Frankfurt, Germany

    Background/Purpose: Fluctuations in disease activity due to short-term situational effects and measurement errors are important considerations for evaluation of individual clinically meaningful therapeutic response in…
  • Abstract Number: 2282 • 2017 ACR/ARHP Annual Meeting

    The Childhood Arthritis and Rheumatology Research Alliance Start Time Optimization of Biologic Therapy in Polyarticular JIA Study: Interim Report of Baseline Patient Characteristics and Treatment Choices

    Sarah Ringold1, George A. Tomlinson2, Pamela F. Weiss3, Laura E. Schanberg4, Brian M. Feldman5, Mary Ellen Riordan6, Anne C. Dennos7, Vincent Del Gaizo8, Katherine Murphy9 and Yukiko Kimura6, 1Seattle Children's Hospital, Seattle, WA, 2Medicine, Mount Sinai Hospital, Toronto, ON, Canada, 3Division of Rheumatology, Center for Pediatric Clincial Effectiveness, Children's Hospital of Philadelphia, Philadelphia, PA, 4Pediatrics, Duke University Medical Center, Durham, NC, 5Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada, 6Hackensack University Medical Center, Hackensack, NJ, 7Duke Clinical Research Institute, Durham, NC, 8Parent Partner, Whitehouse Station, NJ, 9Parent Partner, San Francisco, CA

    Background/Purpose: Despite the many available new and effective treatments for polyarticular JIA (P-JIA), there is significant variation in the timing of when biologic medications are…
  • Abstract Number: 2290 • 2017 ACR/ARHP Annual Meeting

    Comparing Effectiveness of Early Initiation of Biologic Treatment for Newly Diagnosed Juvenile Idiopathic Arthritis Using a Novel Statistics Causal Inference Method Applied to Observational Data

    Bin Huang1, Esi Morgan2, Chen Chen2, Jinzhong Liu2, Michelle Adams2, Timothy Beukelman3, Hermine I. Brunner4 and Daniel J Lovell5, 1Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2Cincinnati Children's Hospital, Cincinnati, OH, 3Pediatric Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 5PRCSG, Cincinnati, OH

    Background/Purpose: We compare the effectiveness of two approaches to treat Juvenile idiopathic arthritis (JIA): early combination of biologic and non-biologic disease modifying anti rheumatic drugs…
  • Abstract Number: 2785 • 2017 ACR/ARHP Annual Meeting

    Serious Infections Associated with Tofacitinib in Rheumatoid Arthritis Patients Previously Treated with Methotrexate

    Marina Amaral de Avila Machado1, Cristiano S. Moura2, Steve Ferreira Guerra1, Jeffrey R. Curtis3, Michal Abrahamowicz4, Hassan Behlouli1 and Sasha Bernatsky5, 1Department of Medicine, McGill University Health Centre, Montreal, QC, Canada, 21Division of Clinical Epidemiology, McGill University Health Centre, Montreal, QC, Canada, 3Rheumatology & Immunology, University of Alabama at Birmingham, Birmingham, AL, 4Department of Medicine, McGill University Health Centre, Montreak, QC, Canada, 5Divisions of Rheumatology and Clinical Epidemiology, McGill University Health Centre, Montreal, QC, Canada

    Background/Purpose: Little is known about the real-world safety of tofacitinib, an oral Janus kinase inhibitor. We compared serious infections associated with tofacitinib, disease-modifying antirheumatic drugs…
  • Abstract Number: 47 • 2017 Pediatric Rheumatology Symposium

    Baseline characteristics of the first 123 patients enrolled in the Childhood Arthritis and Rheumatology Research Alliance Start Time Optimization of Biologic Therapy in Polyarticular JIA comparative effectiveness study

    Sarah Ringold1, George A. Tomlinson2, Pamela F. Weiss3, Laura E. Schanberg4, Brian M. Feldman5, Mary Ellen Riordan6, Anne C. Dennos7, Vincent Del Gaizo8, Kate Murphy9, Yukiko Kimura6 and the CARRA Registry Investigators, 1Seattle Children's Hospital, Seattle, WA, 2Medicine, Mount Sinai Hospital, Toronto, ON, Canada, 3Division of Rheumatology, Center for Pediatric Clincial Effectiveness, Children's Hospital of Philadelphia, Philadelphia, PA, 4Pediatrics, Duke Medical Center, Durham, NC, 5Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada, 6Hackensack University Medical Center, Hackensack, NJ, 7Duke Clinical Research Institute, Durham, NC, 8Parent Partner, Whitehouse Station, NJ, 9Patient Partner, San Francisco, CA

    Background/Purpose: Many new effective treatments for polyarticular JIA (p-JIA) are available, but there is significant variation among pediatric rheumatologists in the timing of when biologic…
  • Abstract Number: 946 • 2016 ACR/ARHP Annual Meeting

    Comparative Effectiveness of Second-Line Treatment Strategies for Lyme Arthritis in Children

    Daniel B. Horton1, Alysha J. Taxter2, Brandt Groh3, David D. Sherry4 and Carlos D. Rosé5, 1Pediatrics, Division of Pediatric Rheumatology, Rutgers Robert Wood Johnson Medical School, Rutgers Biomedical and Health Sciences, New Brunswick, NJ, 2Pediatrics, Brenner Children's Hospital, Wake Forest Baptist Medical Center, Winston-Salem, NC, 3Pediatrics, Penn State Milton S. Hershey Medical Center, Hershey, PA, 4Pediatrics, Children's Hospital of Philadelphia, Division of Pediatric Rheumatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 5Pediatrics, Division of Rheumatology, Nemours/A.I. duPont Hospital for Children, Thomas Jefferson University, Wilmington, DE

    Background/Purpose:  First-line treatment for Lyme arthritis is fairly standardized, but second-line strategies are more variable. We compared the effectiveness of oral antibiotics, intra-articular glucocorticoid injections (IAGC),…
  • Abstract Number: 1999 • 2016 ACR/ARHP Annual Meeting

    Claims-Based Analysis of Cost-Effectiveness Among Patients with Rheumatoid Arthritis Who Switched from a Tumor Necrosis Factor Inhibitor to Another Targeted Disease-Modifying Antirheumatic Drug

    Machaon Bonafede1, Wenhui Wei2, Chieh-I Chen3, Donna McMorrow1, Stefano Fiore4, Jonathan Fay3, Toshio Kimura3 and Jeffrey R. Curtis5, 1Truven Health Analytics, Cambridge, MA, 2Sanofi US, Inc., Bridgewater, NJ, 3Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 4Sanofi Genzyme, Bridgwater, NJ, 5Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Patients with rheumatoid arthritis (RA) who have an inadequate response to a tumor necrosis factor inhibitor (TNFi) can switch to another targeted disease-modifying antirheumatic…
  • Abstract Number: 2224 • 2015 ACR/ARHP Annual Meeting

    Tailored, Online Education on Comparative Effectiveness Studies in Rheumatoid Arthritis: Success in Improving Knowledge and Clinical Decisions

    Nimish Mehta, Emilie McCardell and Kathleen Geissel, Medscape, LLC, New York, NY

    Background/Purpose: Analysis of past educational activities on comparative effectiveness studies in RA identified different educational needs for varying segments of rheumatologists – from interpretation of…
  • Abstract Number: 2745 • 2015 ACR/ARHP Annual Meeting

    Real World Evaluation of Patients with Rheumatoid Arthritis Initiating Tofacitinib Vs. Adalimumab and Etanercept

    Benjamin Chastek1, James Harnett2, Jeffrey R. Curtis3, Robert Gerber4, David Gruben4, Rui Song5 and Andrew Koenig6, 1Optum Insight, Eden Prairie, MN, 2Pfizer Inc, New York, NY, 3University of Alabama at Birmingham, Birmingham, AL, 4Pfizer Inc, Groton, CT, 5Optum Insight, Reston, VA, 6Pfizer Inc, Collegeville, PA

    Background/Purpose:  In November 2012, the first oral Janus kinase (JAK) inhibitor tofacitinib was approved in the US for the treatment of RA with or without…
  • Abstract Number: 3095 • 2015 ACR/ARHP Annual Meeting

    Initial Results of a Pilot Juvenile Localized Scleroderma (jLS) Comparative Effectiveness Study

    Suzanne C. Li1, Kathryn S. Torok2, Sandy D. Hong3, Polly J. Ferguson4, C. Egla Rabinovich5, Mara L Becker6, Fatma Dedeoglu7, Maria F. Ibarra8, Robert C. Fuhlbrigge9,10, Katie G. Stewart11, Marilynn G. Punaro11, Thomas Mason II12, Elena Pope13, Ronald Laxer14, Gloria C. Higgins15,16 and Brian Feldman17, 1Pediatrics, Joseph M Sanzari Children’s Hospital, Hackensack University Medical Center, Hackensack, NJ, 2Pediatric Rheumatology, Univ of Pittsburgh Med Ctr, Pittsburgh, PA, 3Pediatrics-Rheumatology, U of Iowa Children's Hosp, Iowa City, IA, 4Dept of Pediatrics--Rheum, University of Iowa, Iowa City, IA, 5Pediatric Rheumatology, Duke Univ Med Ctr, Durham, NC, 6Rheumatology, Children's Mercy Kansas City, Kansas City, MO, 7Rheumatology, Boston Children's Hospital, Boston, MA, 8Pediatric Rheumatolgy, Children's Mercy Hospital, Kansas City, MO, 9Program in Rheumatology, Division of Immunology, Boston Children’s Hospital, Boston, MA, 10Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 11Pediatric Rheumatology, Texas Scottish Rite Hospital, Dallas, TX, 12Rheumatology, Mayo Clinic, Rochester, MN, 13Dermatology, Hospital for Sick Children, Toronto, ON, Canada, 14Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada, 15Pediatric Rheumatology OSU, Nationwide Childrens Hosp, Columbus, OH, 16Pediatric Rheumatology Ohio State University, Nationwide Childrens Hospital, Columbus, OH, 17Division of Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada

    Background/Purpose:   Juvenile localized scleroderma (jLS) is a chronic inflammatory and fibrosing disease that causes severe morbidity, including growth defects, cosmetic deformities, seizures and arthropathy.…
  • 1
  • 2
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology